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Formation of Polyethylene Glycol Particles Using a Low-Temperature Supercritical Assisted Atomization Process
Hsien-Tsung Wu1, Hong-Ming Tsai2, Tsung-Hsuan Li3
1Department of Chemical Engineering, Ming Chi University of Technology 84 Gungjuan Rd., Taishan Dist., New Taipei City 24301, Taiwan. stwu@mail.mcut.edu.tw.
Low-temperature supercritical assisted atomization (LTSAA) produced fine polyethylene glycol (PEG) microparticles. Optimal conditions yielded spherical, non-aggregated PEG particles suitable for drug delivery formulations.
Area of Science:
- Materials Science
- Chemical Engineering
- Pharmaceutical Technology
Background:
- Polyethylene glycol (PEG) is a versatile polymer with applications in drug delivery.
- Controlling particle size and morphology is crucial for effective drug formulations.
- Supercritical fluid technology offers precise control over particle formation.
Purpose of the Study:
- To investigate the preparation of polyethylene glycol (PEG) microparticles using low-temperature supercritical assisted atomization (LTSAA).
- To determine the key process parameters influencing PEG particle size and characteristics.
- To evaluate the potential of LTSAA-produced PEG particles as carriers for controlled drug delivery.
Main Methods:
- Utilized low-temperature supercritical assisted atomization (LTSAA) with carbon dioxide and acetone.
- Systematically varied PEG solution concentration, CO2 flow rate, and temperature parameters.
- Analyzed particle size, morphology, and crystallinity using techniques like X-ray and differential scanning calorimetry.
Main Results:
- Achieved spherical, non-aggregated PEG particles with a mean size of 1.7-3.2 µm.
- Identified optimal conditions: low PEG concentration, low precipitator temperature, and low PEG molecular weight.
- Demonstrated that LTSAA-treated PEG exhibits reduced crystallinity, controllable by precipitator temperature.
Conclusions:
- LTSAA is an effective method for producing fine PEG microparticles.
- Optimized process parameters enable control over particle size and properties.
- LTSAA-derived PEG microparticles show promise for developing advanced drug-controlled formulations.
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